Transcript #00014566 (NM_144599.4, NIPA1 gene)

Transcript name transcript variant 1
Gene name NIPA1 (non imprinted in Prader-Willi/Angelman syndrome 1)
Chromosome 15
Transcript - NCBI ID NM_144599.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_653200.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

42 entries on 1 page. Showing entries 1 - 42.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-25_*5550[2] r.= p.=
?/. - c.39_47del r.(?) p.(Ala14_Ala16del)
-?/. - c.39_47del r.(?) p.(Ala14_Ala16del)
?/. - c.42_47dup r.(?) p.(Ala15_Ala16dup)
-?/. - c.42_47dup r.(?) p.(Ala15_Ala16dup)
-?/. - c.42_47dup r.(?) p.(Ala15_Ala16dup)
-?/. - c.42_47dup r.(?) p.(Ala15_Ala16dup)
-?/. - c.42_47dup r.(?) p.(Ala15_Ala16dup)
-/. - c.45_47del r.(?) p.(Ala16del)
-?/. - c.45_47del r.(?) p.(Ala16del)
-/. - c.45_47del r.(?) p.(Ala16del)
-/. - c.45_47del r.(?) p.(Ala16del)
?/. - c.45_47dup r.(?) p.(Ala16dup)
?/. - c.45_47dup r.(?) p.(Ala16dup)
-?/. - c.45_47dup r.(?) p.(Ala16dup)
-?/. - c.45_47dup r.(?) p.(Ala16dup)
-?/. - c.75C>T r.(?) p.(Pro25=)
?/. - c.88_114dup r.(?) p.(Leu30_Ser38dup)
-?/. - c.109G>A r.(?) p.(Val37Met)
+/. - c.134C>G r.(?) p.(Thr45Arg)
?/. - c.139G>A r.(?) p.(Val47Met)
?/. - c.242T>C r.(?) p.(Ile81Thr)
-?/. - c.242T>C r.(?) p.(Ile81Thr)
?/. - c.257C>G r.(?) p.(Ala86Gly)
-?/. - c.291C>G r.(?) p.(Pro97=)
-?/. - c.291C>G r.(?) p.(Pro97=)
-?/. - c.312G>A r.(?) p.(Pro104=)
-?/. - c.312G>A r.(?) p.(Pro104=)
-?/. - c.312G>A r.(?) p.(Pro104=)
+/. - c.316G>A r.(?) p.Gly106Arg
-/. - c.317+1421G>A r.(=) p.(=)
-/. - c.441A>G r.(?) p.(Thr147=)
-/. - c.441A>G r.(?) p.(Thr147=)
-/. - c.441A>G r.(?) p.(Thr147=)
?/. - c.484G>A r.(?) p.(Val162Met)
-?/. - c.537C>T r.(?) p.(Ile179=)
?/. - c.607G>A r.(?) p.(Val203Met)
+/. - c.731A>G r.(?) p.(Gln244Arg)
-?/. - c.753G>C r.(?) p.(Ala251=)
-?/. - c.801G>A r.(?) p.(Val267=)
-?/. - c.*5331T>G r.(=) p.(=)
-?/. - c.*5331T>G r.(=) p.(=)
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